The American Psychiatric Association has just announced that Asperger’s Syndrome will be dropped from the manual used by psychiatrists to diagnose patients with medical disorders.
Asperger’s and other similar disorders will now be lumped under the label ‘autism spectrum disorder.’ Patients and their friends and families are worried that the removal of the term from official usage could further exacerbate the impact of the disorder for some sufferers.
But what does it mean to be living with Asperger’s syndrome? What does it feel like to fall on the autism spectrum? This beautiful post will help you understand the world from a different point of view.
By ANONYMOUS
Imagine for a moment a person who has grown up in a family where they only ever had pet dogs. Their friends and neighbours had pet dogs… all different breeds, colours and temperaments, but still, fundamentally…. dogs. They all went to the dog park together every afternoon and always had a raucously good time. They had never, ever, ever seen a cat. Not once.
Then one day they stumble upon an adorable looking creature that is cute, furry, has a black wet nose, four paws and whiskers and for all intents and purposes, looks exactly like the type of friendly, willing to please dog they had known and loved all their lives. Its tail is waving to and fro in what is perceived to be a welcoming gesture so they go over, ruffle up its soft fur and attempt to roll it over to scratch its belly, anticipating their affectionate gesture will be delightfully received. Only it’s not a dog, it’s a cat, and their interaction is interpreted very differently. Lets just say, fur will fly… and it will fly furiously.
Welcome to the world of a child with Asperger’s Syndrome. A solitary cat, surviving in a room full of boisterous dogs. Its every move being analysed, interpreted and modified based on the framework of rules, behavioural patterns and ingrained habits of the canine species. And as a result, being disastrously misunderstood.
Top Comments
Theres CCHR documentaries called ."Diagnostic and statistical manual". "How psychiatric drugs can kill your child". "The marketing of madness" "Pescription: suicide?" "Psychiatry No science No cures" CCHR stands for citizens commission on Human Rights
Hi,
I go to playgroup with a boy who I think has aspergers. His mum has always compared him to my daughter who is the same age. She at one point had booked an appointment to see a paedatrician to look into whether he has aspergers but cancelled and not rebooked. He is 3.
The question is - would looking into this and getting a diagnosis at this age make much difference to his long term wellbeing? I have encouraged his mum to get him assessed - but she has family telling her that her son is normal. I strongly suspect that her husband has Aspergers.
Thanks
A guy I was kind of seeing had a 3 year old who had been diagnosed and had some speech path and other stuff, but his idiot parents never followed it through. I often wonder about how he's going now. I'd be encouraging her to take him. And take his Dad along too - it may help seeing what Dad is like.
Absolutely. The earlier the identification the quicker the intervention can begin. There is a significant amount of research that demonstrates that early intervention is critical. Maybe sitting with your friend over a cup of tea and looking at some of the Autism Aust. Websites that talk about the different types of services that are available would help her feel following up is worthwhile.
The diagnostic process is long and very very stressful. She may need your support with the process let alone the outcome.
Yep, early diagnosis is crucial. Early intervention funding cuts off at 7yrs which means children can miss out on valuable specialist services such as speech therapy. It can also take a long time to get a diagnosis which can result in children falling behind at school before funding for extra support is in place.
Early intervention funding cuts off at 7yrs so the earlier the diagnosis the better - later could mean missing out on valuable specialist services such as speech therapy. Also it can take a long time for diagnosis which can mean children fall behind at school while no funding for assistance is in place. Early diagnosis is vital :)